A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564191



Internal ID18862472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:32901167..32960383hg38UCSC Ensembl
Innerchr18:30481131..30540347hg19UCSC Ensembl
Innerchr18:28735129..28794345hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3859217
hg1959217
hg1859217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060448
Supporting Variants
Samples
Known GenesCCDC178
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564191
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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